EP1336473B1 - Film de resine etire multicouche - Google Patents
Film de resine etire multicouche Download PDFInfo
- Publication number
- EP1336473B1 EP1336473B1 EP01965694A EP01965694A EP1336473B1 EP 1336473 B1 EP1336473 B1 EP 1336473B1 EP 01965694 A EP01965694 A EP 01965694A EP 01965694 A EP01965694 A EP 01965694A EP 1336473 B1 EP1336473 B1 EP 1336473B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- multilayered
- resin film
- stretched resin
- back layer
- stretched
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
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- 238000005299 abrasion Methods 0.000 description 1
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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/16—Layered products comprising a layer of synthetic resin specially treated, e.g. irradiated
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
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- B32B2607/00—Walls, panels
- B32B2607/02—Wall papers, wall coverings
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
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- Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
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-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
Definitions
- JP-A-8325383 relates to the production of a thermoplastic water absorbing resin.
- the resin is produced by reacting a specific polyalkylene oxide containing polyethylene oxide mixed with polypropylene oxide and a low-molecular diol with a diisocyanate compound and then mixing the resultant reactional product with a polyolefin-based resin.
- WO 99/59813 describes a stretched film of a thermoplastic resin which comprises (A) a stretched film substrate layer containing 40 to 85 wt.% of a thermoplastic resin and 60 to 15 wt.% of an inorganic or organic fine powder and, laminated on at least one surface thereof, (B) at least one stretched film surface layer containing 30 to 90 wt.% of a thermoplastic resin and 70 to 10 wt.% of an inorganic or organic fine powder which has an average particle diameter smaller than that of the inorganic or organic fine powder contained in the substrate layer (A), and it has a porosity of 5 to 60 %.
- 11-293600 proposes a wallpaper in which a PET film, PP film, or the like is laminated between the backing paper and a foam gelled PVC material.
- a PET film, PP film, or the like is laminated between the backing paper and a foam gelled PVC material.
- the cost of recycling is increased and in that the quality of the recycled resin material drops, rendering these wallpapers impractical.
- disposed wallpaper is still being mostly buried or incinerated, and not recycled.
- the present invention provides a multilayered-stretched resin film characterized in that on the back surface of a printable front layer (A) comprising a thermoplastic resin, an inorganic fine powder, and/or an organic filler is laminated a back layer (B) comprising a surface-treated inorganic fine powder and a thermoplastic resin comprising a hydrophilic thermoplastic resin, and in that the peel strength of back layer (B) is from 10 to 200 g/cm.
- back layer (B) comprises from 3 to 200 weight parts of hydrophilic thermoplastic resin per 100 weight parts of nonhydrophilic thermoplastic resin.
- the thermoplastic resin is desirably an olefin-based resin, olefin-based thermoplastic elastomer, or a mixture thereof.
- the olefin thermoplastic elastomer employed desirably has a melting point of greater than or equal to 160°C.
- from 10 to 300 weight parts of olefin-based thermoplastic elastomer are desirably incorporated per 100 weight parts of olefin-based resin.
- the hydrophilic thermoplastic resin is desirably an alkylene oxide polymer.
- the outer surface of the inorganic fine powder employed in back layer (B) is desirably treated with at least one selected from the group consisting of anionic surfactants, cationic surfactants, nonionic surfactants, and antistatic agents.
- the liquid water-absorption volume of back layer (B) is desirably from 6 to 50 mL/m 2 as measured by Japan TAPPI No. 51-87.
- the multilayered-stretched resin film of the present invention comprises at least a front layer (A) and a back layer (B).
- Front layer (A) comprises a thermoplastic resin, an inorganic fine powder, and/or an organic filler.
- Back layer (B) comprises thermoplastic resin comprising a hydrophilic thermoplastic resin, and a surface-treated inorganic fine powder.
- Front layer (A) and back layer (B) desirably comprise thermoplastic resin as an olefin-based thermoplastic elastomer.
- thermoplastic resin employed in front layer (A) is not specifically limited.
- the thermoplastic resin of preference incorporates an olefin-based thermoplastic elastomer as the thermoplastic resin. So long as an olefin-based thermoplastic elastomer is incorporated, neither the type nor composition of the other resins contained in the front layer (A) are specifically limited.
- branched ethylene linear polyethylene, high-density polyethylene, and linear low-density polyethylene with a density of from 0.89 to 0.97 g/cm 3 and a melt flow rate (190°C, 2.16 kg load) of from 1 to 10 g/10 min; propylene homopolymer, propylene ethylene copolymer, propylene 1-butene copolymer, propylene ethylene 1-butene copolymer, propylene 4-methyl-1-pentene copolymer, propylene 3-methyl-1-pentene copolymer, poly(1-butene), poly(4-methyl-1-pentene), and propylene ethylene 3-methyl-1-pentene copolymer with a melt flow rate (230°C, 2.16 kg load) of from 0.2 to 20 g/10 min.
- propylene homopolymers propylene ethylene random copolymers, high-density polyethylene, and linear low-density polyethylene are preferred because they are inexpensive and afford good molding properties.
- Ethylene-based rubbers typified by EPDM are examples of the above-described olefin-based elastomers.
- Examples of olefin-based resins are polyethylene and propylene-based resins.
- the melting point (DSC peak temperature) of the olefin-based thermoplastic elastomer employed in front layer (A) and back layer (B) is desirably greater than or equal to 160°C, preferably from 165 to 180°C.
- front layer (A) is imparted with good suitability for embossing, the film rigidity required for application to the wall surface, and flexibility to absorb unevenness on the wall surface following application. Further, it becomes easy to ensure that the porosity of back layer (B) is greater than that of front layer (A) so that peeling starts in back layer (B).
- Additives such as coloring pigments, flame retardants, oxidation inhibitors, dispersing agents, mildew-combatting agents, antibacterial agents, and UV-stabilizers may be added as needed to the above-described olefin-based thermoplastic elastomer and thermoplastic resin.
- weight parts of the olefin-based thermoplastic elastomer are desirably incorporated per 100 weight parts of olefin-based resin into front layer (A).
- An inorganic fine powder and/or an organic filler are employed in front layer (A).
- the type of inorganic fine powder is not specifically limited.
- examples are heavy calcium carbonate, light calcium carbonate, clay, talc, titanium dioxide, barium sulfate, zinc oxide, magnesium oxide, diatomaceous earth, and silicon oxide with an average particle diameter of from 0.1 to 3 micrometers.
- light and heavy calcium carbonate, clay, diatomaceous earth, and titanium dioxide are preferred due to low cost and good formability of voids generated during shaping by stretching.
- the type of organic filler is not specifically limited. However, a resin differing from the main component thermoplastic resin and having an average particle diameter of from 0.1 to 3 micrometers following dispersion is desirable.
- the thermoplastic resin film is an olefin-based resin film
- examples of the organic filler are polyethylene terephthalate, polybutylene terephthalate, polycarbonate, nylon 6, nylon 6,6, cyclic olefin homopolymers, and copolymers of cyclic olefin and ethylene, with a melting point of from 120 to 300°C or a glass transition temperature of from 120 to 280°C.
- Dispersing agents, oxidation inhibitors, UV-stabilizers, and compatibility-enhancing agents are desirably added in the course of blending and kneading these organic fillers into the olefin-based resins.
- the quantity and type of compatibility-enhancing agent selected is particularly important because it determines the shape of the particles of the organic filler.
- front layer (A) comprises 10 to 60 weight percent of organic filler and/or inorganic fine powder having an average particle diameter of from 0.1 to 3 micrometers and 40 to 90 weight percent of the mixture of olefin-based resin and olefin-based thermoplastic elastomer in front layer (A).
- ink adhesion tends to deteriorate.
- uniform stretching becomes difficult, tears occur in the surface of the stretched film, and practical use tends to be precluded.
- average particle diameter of the inorganic fine powder and/or organic filler is less than 0.1 micrometer, secondary aggregation occurs due to poor dispersion in the thermoplastic resin, numerous protrusions are present on the surface, and high-precision printing tends to be precluded.
- high-precision printing tends to be precluded.
- the flatness of the surface decreases and, similarly, high-precision printing tends to be precluded.
- thermoplastic resin that do not satisfy such conditions are referred to as nonhydrophilic thermoplastic resins.
- thermoplastic resin is a concept encompassing both hydrophilic thermoplastic resins and nonhydrophilic thermoplastic resins.
- a surface-treated inorganic fine powder is employed in back layer (B).
- surface-treated inorganic fine powders are obtained by treating heavy calcium carbonate with a water-soluble anionic, cationic, or nonionic surfactant having an average molecular weight of from 1,000 to 150,000 during wet comminution; treating heavy calcium carbonate with an anionic, cationic, or nonionic antistatic agent during wet comminution; and treating heavy calcium carbonate in two stages with the above-listed surfactants and antistatic agents.
- the multilayered-stretched resin film of the present invention comprises front layer (A) and back layer (B) satisfying the conditions of the present invention, it may also comprise other layers.
- one or more intermediate layers (C) may be provided between front layer (A) and back layer (B).
- intermediate layer (C) desirably has a porosity roughly identical to that of back layer (B).
- the porosities of the individual layers desirably satisfy the following relations: Back layer B > intermediate layer ( C ) > front layer A Further, the difference in porosity between back layer (B) and front layer (A) is desirably greater than or equal to 20 percent.
- the thickness of the multilayered-stretched resin film of the present invention is desirably from 30 to 500 micrometers, preferably from 40 to 400 micrometers. It is possible to achieve a thickness of over 1 mm by adhesion with various adhesives.
- a ratio of thickness (A)/(B) of front layer (A) to back layer (B) of (1 to 7)/(9 to 3) is desirable from the perspectives of film strength, suitability for printing, ease of embossing, and embossing reversion.
- the thickness ratio of back layer (B) is less than 30 percent, the embossing tends not to take hold. Further, the amount of water-soluble adhesive absorbed is inadequate, causing the adhesive to tend to dry poorly.
- an intermediate layer (C) it is desirable to include the thickness of layer (C) together with that of back layer (B) when weighing these considerations.
- a surface protective layer comprised of a transparent resin layer can be formed on the outermost layer.
- the surface protective layer functions both to protect the outer surface layer and to impart a sense of perslective to the lower layer printing or embossed designs. Accordingly, even when employing the multilayered-stretched resin film of the present invention in decorative panels and fire-retardant composite sheets, a surface protective layer is particularly useful.
- Adhesive may be directly applied to the back side of the multilayered-stretched resin film of the present invention, which may then be directly adhered to wooden wall materials, gypsum board, various composition materials (including resin-treated decorative panels and gypsum boards), and metal sheets such as iron and aluminum sheets.
- wooden wall materials gypsum board, various composition materials (including resin-treated decorative panels and gypsum boards), and metal sheets such as iron and aluminum sheets.
- the adhesive employed to hang the multilayered-stretched resin film of the present invention is not specifically limited; water-soluble adhesives, carbohydrate adhesives, synthetic resin adhesives, and the like may be employed.
- the adhesive may be soluble in a solvent or water. From the perspectives of ease of operation and stability problems (toxicity, fires, and the like due to vaporizing of solvent), the use of a water-soluble adhesive is preferred.
- a water-soluble adhesive such as a starch or a derivative thereof, polyacrylic acid, polyacryl amide, polyethylene oxide, polyvinyl alcohol, carboxymethyl cellulose (CMC), vinyl acetate, or polyvinyl amide is desirable from the perspectives of application and adhesion when hanging the multilayered-stretched resin film of the present invention on a wall or the like.
- Starches and their derivatives are the adhesives of preference.
- water-absorbant back layer (B) remains on the wall surface.
- a water-soluble adhesive is directly coated on back layer (B) of the multilayered-stretched resin film of the present invention, adequate adhesion is achieved by hanging directly onto the back layer (B) remaining on the wall surface. That is, it is not necessary to first peel off the back layer (B) remaining on the wall before hanging a new multilayered-stretched resin film.
- the back layer (B) remaining on the wall surface can be used for rehanging any number of times.
- compositions (A) and (B) were prepared, they were melted and kneaded in two extruders set to 250°C, the two compositions were laminated in a die, the laminate was extrusion molded and cooled to 70°C with a cooling device to obtain a two-layer unstretched sheet.
- both surfaces of the stretched films obtained were corona discharge treated at 50 W/m 2 min using a discharge processor (made by Kasuga Electronics (Ltd.)) to obtain multilayered-stretched resin films.
- the porosities of the individual layers, overall porosities and densities in the multilayered-stretched resin films obtained are given in Table 4.
- the contact angles of water of the back layers (B) of the individual stretched resin films prepared in Examples 1 to 6 and Comparative Examples 1 and 2 were measured ten times with a contact angle meter (Model CA-D, made by Kyowa Interface Science Co., Ltd.) using ion-exchange water and the average values were calculated.
- the liquid water absorption volume of the back layer (B) side of the individual multilayered-stretched resin films prepared in Examples 1 to 6 and Comparative Examples 1 to 4 were measured in accordance with Japan TAPPI No. 51-87 (Paper Pulp Technology Association, Paper Pulp Test Method No.51-87, Bristow method). That is, a Bristow Tester II made by Kumagaya Riki Kogyo (K.K.) was employed to add dropwise 20 microliters of a 1:20 mixed solution of red water-based ink in ion-exchange water in a nonpressurized state, and the liquid water absorption volume was obtained at 50 (T 1/2 ms).
- Adhesive tape product name "Cellotape” made by Nichiban (K.K.) was applied to the ink surface of individual gravure printed multilayered-stretched resin films and pressed well into place. The adhesive tape was then peeled off at an angle of 90 degrees at a constant rate and ink removal was measured based on the following scale:
Landscapes
- Laminated Bodies (AREA)
Claims (18)
- Film de résine étiré multicouche caractérisé en ce que, sur la face postérieure d'une couche antérieure imprimable (A) comprenant une résine thermoplastique, une fine poudre inorganique, et/ou une charge organique, est appliquée une couche postérieure (B) comprenant une fine poudre inorganique ayant reçu un traitement de surface et une résine thermoplastique comprenant une résine thermoplastique hydrophile, et en ce que la résistance au pelage de la couche postérieure (B) varie de 10 à 200 g/cm, dans lequel la résistance au pelage est déterminée en appliquant un ruban adhésif (nom du produit « Cellotape » de la société Nichiban (K. K.)) sur la face correspondant à la couche postérieure (B) du film de résine étiré multicouche individuel, puis en découpant dans ce dernier un morceau de 10 mm de large et de 100 mm de long, puis en utilisant, vingt-quatre heures plus tard, un dispositif d'essai de traction (nom du produit « Autograph », de la société Shimadzu Corporation) pour arracher le ruban dans les conditions suivantes : angle de 180 degrés et vitesse de traction de 1 000 mm/min, afin de pouvoir mesurer la résistance à la traction.
- Film de résine étiré multicouche selon la revendication 1, dans lequel le volume d'absorption d'eau liquide, comme mesuré selon la norme japonaise TAPPI n°51-87, de ladite couche postérieure (B) varie de 6 à 50 ml/m2.
- Film de résine étiré multicouche selon la revendication 1 ou la revendication 2, dans lequel ladite résine thermoplastique est une résine à base d'oléfine, un élastomère thermoplastique à base d'oléfine, ou un mélange d'une résine à base d'oléfine et d'un élastomère thermoplastique à base d'oléfine.
- Film de résine étiré multicouche selon la revendication 3, dans lequel ledit mélange d'une résine à base d'oléfine et d'un élastomère thermoplastique à base d'oléfine comprend de 10 à 300 parties en poids d'élastomère thermoplastique à base d'oléfine pour 100 parties en poids de résine à base d'oléfine.
- Film de résine étiré multicouche selon la revendication 3 ou la revendication 4, dans lequel le point de fusion dudit élastomère thermoplastique à base d'oléfine est supérieur ou égal à 160 °C.
- Film de résine étiré multicouche selon la revendication 1, dans lequel ladite couche postérieure (B) comprend de 3 à 200 parties en poids de ladite résiste thermoplastique hydrophile pour 100 parties en poids de résine thermoplastique non hydrophile.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 6, dans lequel ladite résine thermoplastique hydrophile est un polymère d'oxyde d'alkylène.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 7, dans lequel la surface de la fine poudre inorganique utilisée dans la couche postérieure (B) est traitée au moyen d'au moins un composé choisi dans le groupe constitué par les tensioactifs anioniques, les tensioactifs cationiques, les tensioactifs non ioniques et les agents antistatiques.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 8, dans lequel la porosité dudit film de résine étiré multicouche varie de 10 à 60 pour cent.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 9, dans lequel la porosité de la couche postérieure (B) est supérieure à la porosité de la couche antérieure (A).
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 10, dans lequel l'angle de contact moyen de l'eau sur la couche postérieure (B) varie de 10 à 80 °.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 11, dans lequel la densité du film de résine étiré multicouche varie de 0,4 à 1 g/cm3.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 12, dans lequel le film est préparé en déposant la couche antérieure (A) sur la couche postérieure (B) pour former une structure stratifiée, puis en étirant ladite structure stratifiée.
- Film de résine étiré multicouche selon la revendication 13, dans lequel la couche antérieure (A) et la couche postérieure (B) sont toutes deux étirées dans au moins une direction axiale.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 14, dans lequel la couche antérieure (A) et la couche postérieure (B) sont soumises à un traitement d'oxydation.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 15, dans lequel la couche antérieure (A) est imprimée, puis gaufrée.
- Film de résine étiré multicouche selon l'une quelconque des revendications 1 à 16, dans lequel le film de résine étiré multicouche est destiné à être utilisé comme adhésif, et un adhésif soluble dans l'eau est appliqué sur la couche postérieure (B).
- Film de résine étiré multicouche selon la revendication 17, dans lequel ledit adhésif soluble dans l'eau est choisi dans le groupe constitué de l'amidon, de l'acide polyacrylique, du polyacrylamide, de l'oxyde de polyéthylène, de l'alcool polyvinylique, de la carboxyméthylcellulose, de l'acétate de vinyle et du polyvinylamide.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000286266A JP4448607B2 (ja) | 2000-09-21 | 2000-09-21 | 多層樹脂延伸フィルム |
JP2000286266 | 2000-09-21 | ||
JP2000332690 | 2000-10-31 | ||
JP2000332690 | 2000-10-31 | ||
PCT/JP2001/008100 WO2002024448A1 (fr) | 2000-09-21 | 2001-09-18 | Film de resine etire multicouche |
Publications (3)
Publication Number | Publication Date |
---|---|
EP1336473A1 EP1336473A1 (fr) | 2003-08-20 |
EP1336473A4 EP1336473A4 (fr) | 2006-09-20 |
EP1336473B1 true EP1336473B1 (fr) | 2008-08-27 |
Family
ID=26600376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01965694A Expired - Lifetime EP1336473B1 (fr) | 2000-09-21 | 2001-09-18 | Film de resine etire multicouche |
Country Status (5)
Country | Link |
---|---|
US (2) | US20030219585A1 (fr) |
EP (1) | EP1336473B1 (fr) |
AU (1) | AU2001286270A1 (fr) |
DE (1) | DE60135571D1 (fr) |
WO (1) | WO2002024448A1 (fr) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1553126B1 (fr) * | 2002-07-25 | 2013-12-25 | Yupo Corporation | Bande de resine allongee et etiquette comprenant celle-ci |
US7981503B2 (en) | 2002-07-25 | 2011-07-19 | Yupo Corporation | Stretched resin film and label comprising the same |
US8398306B2 (en) | 2005-11-07 | 2013-03-19 | Kraft Foods Global Brands Llc | Flexible package with internal, resealable closure feature |
US7871696B2 (en) * | 2006-11-21 | 2011-01-18 | Kraft Foods Global Brands Llc | Peelable composite thermoplastic sealants in packaging films |
US7871697B2 (en) | 2006-11-21 | 2011-01-18 | Kraft Foods Global Brands Llc | Peelable composite thermoplastic sealants in packaging films |
US9232808B2 (en) | 2007-06-29 | 2016-01-12 | Kraft Foods Group Brands Llc | Processed cheese without emulsifying salts |
NZ591354A (en) | 2010-02-26 | 2012-09-28 | Kraft Foods Global Brands Llc | A low-tack, UV-cured pressure sensitive acrylic ester based adhesive for reclosable packaging |
ES2739703T3 (es) | 2010-02-26 | 2020-02-03 | Intercontinental Great Brands Llc | Envase que tiene un fijador de cierre reutilizable adhesivo y métodos para este |
CN102971144B (zh) | 2010-06-30 | 2015-04-08 | 优泊公司 | 易剥离性薄膜、模内成型用标签、带标签的树脂成型品、壁纸、不干胶标签以及带标签的容器 |
US9533472B2 (en) | 2011-01-03 | 2017-01-03 | Intercontinental Great Brands Llc | Peelable sealant containing thermoplastic composite blends for packaging applications |
US9919550B2 (en) | 2013-07-25 | 2018-03-20 | Hewlett-Packard Development Company, L.P. | Recording medium and method for making the same |
TWI750611B (zh) | 2019-03-22 | 2021-12-21 | 日商旭化成股份有限公司 | 滅菌用包裝材用不織布 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5422175A (en) * | 1992-06-01 | 1995-06-06 | Toyo Boseki Kabushiki Kaisha | Void-containing composite film of polyester type |
JP3071680B2 (ja) * | 1994-10-24 | 2000-07-31 | 三洋化成工業株式会社 | 吸水性樹脂分散体 |
JPH08325383A (ja) * | 1995-06-02 | 1996-12-10 | Sumitomo Seika Chem Co Ltd | 熱可塑性吸水性樹脂の製造法 |
US5853638A (en) * | 1997-06-27 | 1998-12-29 | Samsung General Chemicals Co., Ltd. | Process for producing stretched porous film |
KR20010043687A (ko) * | 1998-05-20 | 2001-05-25 | 다나베 마사히코 | 열가소성 수지 연신필름 |
WO2001042340A1 (fr) * | 1999-12-07 | 2001-06-14 | Yupo Corporation | Film de resine poreux |
US6623841B1 (en) * | 2000-04-11 | 2003-09-23 | Avery Dennison Corporation | Inherently ink-receptive film substrates |
-
2001
- 2001-09-18 WO PCT/JP2001/008100 patent/WO2002024448A1/fr active IP Right Grant
- 2001-09-18 EP EP01965694A patent/EP1336473B1/fr not_active Expired - Lifetime
- 2001-09-18 DE DE60135571T patent/DE60135571D1/de not_active Expired - Lifetime
- 2001-09-18 AU AU2001286270A patent/AU2001286270A1/en not_active Abandoned
-
2003
- 2003-03-21 US US10/392,812 patent/US20030219585A1/en not_active Abandoned
-
2006
- 2006-11-02 US US11/555,912 patent/US9486986B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
AU2001286270A1 (en) | 2002-04-02 |
US20030219585A1 (en) | 2003-11-27 |
US20070054111A1 (en) | 2007-03-08 |
DE60135571D1 (de) | 2008-10-09 |
WO2002024448A1 (fr) | 2002-03-28 |
EP1336473A4 (fr) | 2006-09-20 |
EP1336473A1 (fr) | 2003-08-20 |
US9486986B2 (en) | 2016-11-08 |
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